Noda, Yoshiteru <br/><br/>
Potentially effective method for fetal gender determination by noninvasive prenatal testing for X-linked disease.  [electronic resource] 

 -  Congenital anomalies  May 2019 
 - 88-92 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1741-4520 
<br/><br/><label>Standard No.: </label>10.1111/cga.12302  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Biomarkers--blood<br/>Cell-Free Nucleic Acids--blood<br/>Chromosomes, Human, X--chemistry<br/>Chromosomes, Human, Y--chemistry<br/>Down Syndrome--blood<br/>Female<br/>Fetus<br/>Genetic Diseases, X-Linked--blood<br/>Heterozygote<br/>Humans<br/>Male<br/>Microsatellite Repeats<br/>Multiplex Polymerase Chain Reaction--methods<br/>Polymorphism, Single Nucleotide<br/>Pregnancy<br/>Pregnancy Trimester, First<br/>Prenatal Diagnosis--methods<br/>Trisomy